Cargando…

Ex Vivo Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study

[Image: see text] Osteoarthritis is an age-related degenerative musculoskeletal disease characterized by loss of articular cartilage, synovitis, and subchondral bone sclerosis. Osteoarthritis pathogenesis is yet to be fully elucidated with no osteoarthritis-specific biomarkers in clinical use. Ex vi...

Descripción completa

Detalles Bibliográficos
Autores principales: Anderson, James R., Phelan, Marie M., Foddy, Laura, Clegg, Peter D., Peffers, Mandy J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7476031/
https://www.ncbi.nlm.nih.gov/pubmed/32701294
http://dx.doi.org/10.1021/acs.jproteome.0c00143
_version_ 1783579640807292928
author Anderson, James R.
Phelan, Marie M.
Foddy, Laura
Clegg, Peter D.
Peffers, Mandy J.
author_facet Anderson, James R.
Phelan, Marie M.
Foddy, Laura
Clegg, Peter D.
Peffers, Mandy J.
author_sort Anderson, James R.
collection PubMed
description [Image: see text] Osteoarthritis is an age-related degenerative musculoskeletal disease characterized by loss of articular cartilage, synovitis, and subchondral bone sclerosis. Osteoarthritis pathogenesis is yet to be fully elucidated with no osteoarthritis-specific biomarkers in clinical use. Ex vivo equine cartilage explants (n = 5) were incubated in tumor necrosis factor-α (TNF-α)/interleukin-1β (IL-1β)-supplemented culture media for 8 days, with the media removed and replaced at 2, 5, and 8 days. Acetonitrile metabolite extractions of 8 day cartilage explants and media samples at all time points underwent one-dimensional (1D) (1)H nuclear magnetic resonance metabolomic analysis, with media samples also undergoing mass spectrometry proteomic analysis. Within the cartilage, glucose and lysine were elevated following TNF-α/IL-1β treatment, while adenosine, alanine, betaine, creatine, myo-inositol, and uridine decreased. Within the culture media, 4, 4, and 6 differentially abundant metabolites and 154, 138, and 72 differentially abundant proteins were identified at 1–2, 3–5, and 6–8 days, respectively, including reduced alanine and increased isoleucine, enolase 1, vimentin, and lamin A/C following treatment. Nine potential novel osteoarthritis neopeptides were elevated in the treated media. Implicated pathways were dominated by those involved in cellular movement. Our innovative study has provided insightful information on early osteoarthritis pathogenesis, enabling potential translation for clinical markers and possible new therapeutic targets.
format Online
Article
Text
id pubmed-7476031
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-74760312020-09-08 Ex Vivo Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study Anderson, James R. Phelan, Marie M. Foddy, Laura Clegg, Peter D. Peffers, Mandy J. J Proteome Res [Image: see text] Osteoarthritis is an age-related degenerative musculoskeletal disease characterized by loss of articular cartilage, synovitis, and subchondral bone sclerosis. Osteoarthritis pathogenesis is yet to be fully elucidated with no osteoarthritis-specific biomarkers in clinical use. Ex vivo equine cartilage explants (n = 5) were incubated in tumor necrosis factor-α (TNF-α)/interleukin-1β (IL-1β)-supplemented culture media for 8 days, with the media removed and replaced at 2, 5, and 8 days. Acetonitrile metabolite extractions of 8 day cartilage explants and media samples at all time points underwent one-dimensional (1D) (1)H nuclear magnetic resonance metabolomic analysis, with media samples also undergoing mass spectrometry proteomic analysis. Within the cartilage, glucose and lysine were elevated following TNF-α/IL-1β treatment, while adenosine, alanine, betaine, creatine, myo-inositol, and uridine decreased. Within the culture media, 4, 4, and 6 differentially abundant metabolites and 154, 138, and 72 differentially abundant proteins were identified at 1–2, 3–5, and 6–8 days, respectively, including reduced alanine and increased isoleucine, enolase 1, vimentin, and lamin A/C following treatment. Nine potential novel osteoarthritis neopeptides were elevated in the treated media. Implicated pathways were dominated by those involved in cellular movement. Our innovative study has provided insightful information on early osteoarthritis pathogenesis, enabling potential translation for clinical markers and possible new therapeutic targets. American Chemical Society 2020-07-23 2020-09-04 /pmc/articles/PMC7476031/ /pubmed/32701294 http://dx.doi.org/10.1021/acs.jproteome.0c00143 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Anderson, James R.
Phelan, Marie M.
Foddy, Laura
Clegg, Peter D.
Peffers, Mandy J.
Ex Vivo Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study
title Ex Vivo Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study
title_full Ex Vivo Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study
title_fullStr Ex Vivo Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study
title_full_unstemmed Ex Vivo Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study
title_short Ex Vivo Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study
title_sort ex vivo equine cartilage explant osteoarthritis model: a metabolomics and proteomics study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7476031/
https://www.ncbi.nlm.nih.gov/pubmed/32701294
http://dx.doi.org/10.1021/acs.jproteome.0c00143
work_keys_str_mv AT andersonjamesr exvivoequinecartilageexplantosteoarthritismodelametabolomicsandproteomicsstudy
AT phelanmariem exvivoequinecartilageexplantosteoarthritismodelametabolomicsandproteomicsstudy
AT foddylaura exvivoequinecartilageexplantosteoarthritismodelametabolomicsandproteomicsstudy
AT cleggpeterd exvivoequinecartilageexplantosteoarthritismodelametabolomicsandproteomicsstudy
AT peffersmandyj exvivoequinecartilageexplantosteoarthritismodelametabolomicsandproteomicsstudy